7 results on '"Prisco, F"'
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2. Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family
3. Benign tyrosinaemia: an 18-year follow-up
4. Late onset of cystinuria in a case of gyrate atrophy
5. Low-protein diet and progression of retinal degeneration in gyrate atrophy of the choroid and retina: A twenty-six-year follow-up
6. Autophagy and NLRP3 inflammasome crosstalk in neuroinflammation in aged bovine brains
7. Diabetes, Sensorineural Deafness, and Mitochondrial DNA Mutation
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